• Title/Summary/Keyword: 화학반응율속

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A Study on the Electrochemical Kinetics of Electrowinning Process of Valuable Metals Recovered from Lithium-ion Batteries (폐리튬이온전지로부터 유가금속 회수를 위한 전해채취 공정 전기화학 반응속도론적 연구)

  • Park, Sung Cheol;Kim, Yong Hwan;Lee, Man Seung;Son, Seong Ho
    • Resources Recycling
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    • v.31 no.5
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    • pp.59-66
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    • 2022
  • To investigate the rate-determining step of nickel, cobalt and copper electrowinning, experiments were conducted by varying the electrolyte temperature and agitation speed using a rotating disc electrode. Analyzing the rate-determining step by calculating the activation energy in the electrowinning process, it was found that nickel electrowinning is controlled by a mixed mechanism (partly by chemical reaction and partly by mass transport), cobalt is controlled by chemical reaction, and copper is controlled by mass transfer. Electrowinning of nickel, cobalt and copper was performed by varying the electrolyte temperature and agitation speed, and the comparison of the current efficiencies was used the determine the rate-determining step.

Reduction Kinetics of Zinc Oxide in EAF Dust (전기로 분진중 아금산화물의 환원속도)

  • Moon Seok Min;Kim Tae Wook;Min Dong Joon
    • Resources Recycling
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    • v.11 no.4
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    • pp.37-43
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    • 2002
  • As the consumption of galvanized steels in cans and automobiles and the quantity of scraps increase, the recycling problems of EAF dust become a important problem. Valuable metals such as Fe, Zn, Pb are of continued interest to metallurgists. To recover the valuable metal and to remove the toxicity of EAF dust, high temperature smelting process is or researching as a pilot scale. The Reduction kinetics of Zn in EAF dust is so important in a view of the economic consideration of the process. In this study, the kinetics behavior of Zn in EAF dust were measured as a point of application in high temperature smelting process. The rate control step in ZnO and franklinite is revealed to be chemical reaction on the reaction surface.

Chlorination Kinetics of Synthetic Rutile with Cl2+CO Gas (Cl2+CO 혼합가스에 의한 합성루타일 염화반응의 속도론적 연구)

  • Hong, Sung-Min;Lee, So-Yeong;Sohn, Ho-Sang
    • Resources Recycling
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    • v.29 no.3
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    • pp.3-10
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    • 2020
  • The chlorination kinetics of synthetic rutile prepared by selective chlorination of ilmenite with Cl2 and CO gas mixture were studied in a fluidized bed. Th e effects of reaction temperature, reaction time, and the ratio of Cl2 and CO partial pressure ($p_{Cl_2}/p_{CO}$) on the conversion rate of TiCl4 were investigated. The conversion rate of TiC4 was low under the high $p_{Cl_2}/p_{CO}$ conditions. Moreover, it was considered that the partial pressure of CO gas was more effective than that of Cl2 gas when comparing the stoichiometric conversion rate and experimental results of high CO partial pressure. Considering the porous structure of particles, the rate controlling step of the chlorination of synthetic rutile was determined to be chemical reaction and the activation energy was calculated as 53.77 kJ/mol.

Studies on the Heat Storage Using the Hydration/Dehydration of the Calcined Dolomite (소성 Dolomite의 수화 및 탈수반응을 이용한 축열에 관한 연구)

  • Lee, Soo-Kag;Lee, Young-Sei;Kim, Jong-Shik
    • Applied Chemistry for Engineering
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    • v.3 no.3
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    • pp.507-515
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    • 1992
  • This study was carried out to investigate the heat-storage/-release characteristics of the thermochemical reaction of the calcined dolomite and steam system for the application of regenerative heat exchangers with the packed bed shape experimental apparatus. The experimental data were obtained at the following conditions ; the hydration temperature was $150-400^{\circ}C$, the dehydration temperature was $700-800^{\circ}C$ and the steam mass flow rates were 294, 430 and 567 g/hr. In the present study, it was found that MgO of the calcined dolomite was not hydrated during the hydration process under the studied experimental conditions. Therefore, MgO of the calcined dolomite can be regard as an inert material. Because the reaction was proceeded from the packed bed input to packed bed output and from wall to center, it could be thought that the rate determining step is not the reaction itself but the heat transfer.

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Kinetics of $N_2H_4-I_2$ Reaction in Sulfuric Acid Media (황산 산성용액중에서의 $N_2H_4-I_2$ 반응의 속도론적 연구)

  • Q. Won Choi;Chuhyun Choe;Wonki Choi;Soonki Lee
    • Journal of the Korean Chemical Society
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    • v.19 no.5
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    • pp.339-342
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    • 1975
  • The rates of consumption of iodine and gas evolution in hydrazine-iodine reaction in the presence of large excess of hydrazine have been studied in the pH range 0.5${\sim}$7. They are the same at very low pH and both increase to respective asymptotic values as pH is increased. The rate of iodine consumption is three orders of magnitude faster than the rate of gas evolution at higher pH. The results are explained by postulating that $N_2H_4$ but not protonated form reacts with iodine and an intermediate, probably $N_2H_2I_2$, is formed which decomposed by first order reaction of rate constant about 1.5${\times}10^{-3}sec^{-1}$ in neutral and weakly acidic solutions.

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Synthesis Characteristics of ZnO Powder from Precursors Composed of Nitrate-Citrate Compounds (Nitrate-Citrate 혼합 전구체로부터 ZnO 입자의 합성반응 특성)

  • Yang, Si Woo;Lee, Seung Ho;Lim, Dae Ho;Yoo, Dong Jun;Kang, Yong
    • Korean Chemical Engineering Research
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    • v.54 no.3
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    • pp.299-304
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    • 2016
  • Characteristics of self-propagating reaction for the preparation of ZnO powder from precursors composed of nitrate and citrate compounds were examined. The ratio of C/N was maintained in range of 0.7~0.8 to initiate the self-propagating reaction between the reducing citrate and oxidizing nitrate groups. The samples were decomposed thermally by using TGA. The sudden decomposition occurred in the range of X > 0.5 in a very short time with a very sharp decrease of mass, indicating that the self-propagating reaction would occur. Friedman, Ozawa-Flynn-Wall and Vyazovkin methods were employed to predict the activation energy, reaction order and frequency factor of the reaction rate in the rate determining step of X < 0.5 range. The activation energy increased with increasing fractional conversion in the range of 46~130 (kJ/min). The reaction order decreased in the range of 2.9~0.9, while the frequency factor increased in the range of 85~278 ($min^{-1}$), respectively, with increasing the rate of temperature increase.

Development of Porous Sorbents for Removal of Hydrogen Sulfide from Hot Coal Gases III. Study on Ferrite-type adsorbent for the Removal of Hydrogen Sulfide

  • Kim, Jong-Saeng;Lee, Young-Soo;Lee, Bok-Jae;Yoo, Kyong-Ok
    • Journal of Environmental Health Sciences
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    • v.17 no.1
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    • pp.39-49
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    • 1991
  • 고온에서 황화수소(H$_{2}$S)를 제거하기 위한 흡착제를 개발할 목적으로 ZnO에 $Fe_{2}O_{3}$를 5~50 atomic %까지 첨가시켜 제조한 다공성 흡착제와 황화수소와의 반응(sulfidation)을 thermogravimetric analyzer (Shimadzu DT-30)로 수행하였으며, 고정층세서 zinc ferrite 흡착제의 흡착능을 측정하였다. 반응온도는723$^{\circ}$K~973$^{\circ}$K범위이며, 반응기체는 황화수소(2vol.%)와 질소와 혼합기체로서 total gas flow rate는 200ml/min으로 고정시켰다. Grain Model을 사용하여 실험데이터를 분석한 결과 전화율이 낮을 때 zinc ferrite와 황화수소 반응의 율속단계는 화학반응이었고 황화수소 농도에 대해 1차 반응이었다. 실험한 흡착제 중 10 atomic %의 $Fe_{2}O_{3}$를 첨가하여 제조한 zinc ferrite형 흡착제가 반응속도, 흡착능, 그리고 재생성면에서 우수한 흡착제로 밝혀졌다.

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Cathodic Polarization Measurements on La0.9Sr0.1MnO3 Electrode for Solid Oxide Fuel Cells

  • Lee, H.Y.;Oh, S.M.
    • Applied Chemistry for Engineering
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    • v.4 no.1
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    • pp.153-161
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    • 1993
  • Cathodic oxygen reduction kinetics on $La_{0.9}Sr_{0.1}MnO_3$ electrode have been examined at $700-900^{\circ}C$ under various oxygen partial pressures. AC impedance and current interruption techniques were employed for the determination of charge transfer resistances for electrochemical oxygen reduction. The $R_{ct}$ values obtained from two different methods were very close each other for $La_{0.9}Sr_{0.1}MnO_3$ electrode. Activation energy for the electrochemical oxygen reduction was found to be 174kJ/mol under atmospheric oxygen pressure. $R_{ct}$ measurements as a function of oxygen partial pressure indicate that the rate-determining step for the electrochemical oxygen reduction on $La_{0.9}Sr_{0.1}MnO_3$ electrode is the charge transfer process.

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Sulfuric Acid Leaching of Manganese from Ferromanganese Dust (황산에 의한 페로망간 집진분 중의 망간 침출)

  • Park, Suji;Sohn, Ho-Sang
    • Resources Recycling
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    • v.24 no.6
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    • pp.24-30
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    • 2015
  • The sulfuric acid leaching of ferromanganese dust was studied. The effect of acid concentration, reaction temperature, stirring rate, particle size and solid to liquid ratio on Mn and Fe extraction in the solution were investigated. It was found that the leaching rate of Mn and Fe increased with increasing reaction temperature and sulfuric acid concentration. Examination of data by shrinking core model suggested that the leaching rate is controlled by chemical reaction at the surface of particle. The activation energy for the leaching reaction of Mn and Fe were calculated to be 79.55 kJ/mol and 77.48 kJ/mol, respectively.

Kinetic Study of Synthesis of Aluminum Nitride Using Carbon Reduction and Subsequent Nitridation Method (탄소환원질화법에 의한 AlN 합성의 속도론적 연구)

  • Park, Hyungkyu;Choi, Youngyoon;Nam, Chulwoo
    • Resources Recycling
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    • v.26 no.3
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    • pp.39-46
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    • 2017
  • AlN powder was prepared by carbon reduction and subsequent nitridation method through lab- scale experiments. AlN powder was synthesized using the mixture of high purity $Al_2O_3$ powder and carbon black at $1,600{\sim}1,700^{\circ}C$ for 0.5~6 hours under nitrogen atmosphere (flow rate of nitrogen gas: $4.7{\times}10^{-6}{\sim}20{\times}10^{-6}m^3/sec$) with variation of charged height of the mixture powder. Experimental results showed that size of the synthesized particles grows with increasing of temperature. The reaction activation energy was calculated as 382 kJ/mol at the temperature range, and it was considered that chemical reaction is the rate determining step. Content of oxygen and nitrogen of the prpared samples were 0.71~0.96 wt% and 30.7~35.1 wt%. The results was similar with those of the commercial AlN product.